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HuagongsheHuagongshe Chemistry Print Report · For research reference only
HRID 1004607Generated: October 25, 2026

1,2-Dimethoxyethane → 6-(Thiophen-2-Yl)Pyridine-3-Carboxylic Acid

https://huagongshe.com/reaction/1004607

Reaction equation

Participants

RoleNameHCIDCharge
Reactant1,2-DimethoxyethaneHCID 8071—
Reactant2-Thiopheneboronic acidHCID 2733960—
ReactantBarium hydroxideHCID 6093286—
Reactant2-Trifluoromethanesulfonyloxy-5-pyridinecarboxylic acidHCID 15411143—
CatalystTetrakis(triphenylphosphine)palladiumHCID 11979704—
SolventWaterHCID 962—
Product6-(Thiophen-2-Yl)Pyridine-3-Carboxylic AcidHCID 15411144—

Reaction Steps

A mixture of 2-trifluoromethanesulfonyloxy-5-pyridine-carboxylic acid (0.442 g, 1.72 mmol), 2-thienylboronic acid (1.56 g, 12.79 mmol), barium hydroxide (0.813 mg, 2.58 mmol), DME (8 mL) and water (1.5 mL) is purged with dry argon. Tetrakis(triphenyl-phosphine) palladium(0) (99.0 mg, 0.086 mmol) is added, and the resultant solution is stirred at 80° C. for 4 hours. The solvents are evaporated in vacuo, and the residue is partitioned between EtOAc and water. The aqueous extract is separated, and extracted with EtOAc. The organic extracts are combined, washed with sat. aq. NaHCO3 and 5% aq. Na2S2O3, dried, (Na2SO4) and the solvent is evaporated in vacuo. The residue is purified by chromatography to afford the title compound.

Provenance & Evidence

DOI10.6084/m9.figshare.5104873.v1
Patent numberUS06051574
Source datasetuspto-grants-2000_04
ORD IDord-decd5796fac84f568afe440fd831a831
Source noteuspto-grants-2000_04